Zhainazarov A B, Doolin R, Herlihy J D, Ache B W
Whitney Laboratory, University of Florida, St. Augustine, Florida 32086, USA.
J Neurophysiol. 2001 Jun;85(6):2537-44. doi: 10.1152/jn.2001.85.6.2537.
Two antagonists of phosphoinositide 3-OH kinases (PI3Ks), LY294002 and Wortmannin, reduced the magnitude of the receptor potential in lobster olfactory receptor neurons (ORNs) recorded by patch clamping the cells in vivo. An antibody directed against the c-terminus of human PI3K-P110 beta detected a molecule of predicted size in the outer dendrites of the ORNs. Two 3-phosphoinositides, PI(3,4)P(2) (1--4 microM) and PI(3,4,5)P(3) (1--4 microM) applied to the cytoplasmic side of inside-out patches taken from cultured lobster ORNs, reversibly activated a Na(+)-gated channel previously implicated in the transduction cascade in these cells. 3-Phosphoinositides were the most effective phosphoinositide (1 microM) in enhancing the open probability of the channel. Collectively, these results implicate 3-phosphoinositides in lobster olfactory transduction and raise the need to consider the 3-phosphoinositide pathway in olfactory transduction.
两种磷酸肌醇3 - 羟基激酶(PI3Ks)拮抗剂,LY294002和渥曼青霉素,降低了通过在体膜片钳记录的龙虾嗅觉受体神经元(ORN)中感受器电位的幅度。一种针对人PI3K - P110β C末端的抗体在ORN的外树突中检测到一个预测大小的分子。将两种3 - 磷酸肌醇,PI(3,4)P(2)(1 - 4 microM)和PI(3,4,5)P(3)(1 - 4 microM)应用于取自培养龙虾ORN的内向外膜片的细胞质侧,可逆地激活了先前与这些细胞转导级联相关的Na(+)门控通道。3 - 磷酸肌醇是增强通道开放概率最有效的磷酸肌醇(1 microM)。总体而言,这些结果表明3 - 磷酸肌醇参与龙虾嗅觉转导,并提出了在嗅觉转导中考虑3 - 磷酸肌醇途径的必要性。